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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1039730Erstellt: 24. Oktober 2026

Tetrahydrofuran → HCID 67270703, Verbindung

https://huagongshe.com/de/reaction/1039730

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt(NE,S)-N-[(2S)-2,3-bis[[tert-butyl(dimethyl)silyl]oxy]propylidene]-2-methylpropane-2-sulfinamideHCID 44239381—
EduktHCID 178418306HCID 178418306—
ProduktHCID 67270703HCID 67270703—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of azeotropically dried (S,E)-N-((S)-2,3-bis(tert-butyldimethylsilyloxy)propylidene)-2-methylpropane-2-sulfinamide (2.3 g, 5 mmol) and 3-(iodomethyl)-THF (1 g, 7 mmol) in dry THF (10 mL) was brought to −78° C. followed by the dropwise addition of tert-butyllithium (6 mL, 11 mmol). A white precipitate was formed. The resulting solution was stirred at −78° C. for 40 min, quenched with sat NH4Cl and extracted with EtOAc. The combined organics were washed with brine, dried over Na2SO4, filtered, concentrated, and chromatographed on silica gel using 0-5% EtOAc/hexanes to afford a colorless oil as (S)-N-((2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(tetrahydrofuran-3-yl)butan-2-yl)-2-methylpropane-2-sulfinamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552181B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-5854fd72d51041fd9d5ce3afe3f767a3
Quellennotizuspto-grants-2013_10